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FIGURE 6 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 6. Mesonemoura diqinga Rehman, Du & Zhao sp. nov. A: Male head and prothorax; B: Cervical gills; C: Male Terminalia, dorsal view; D: Male terminalia, ventral view.
FIGURE 2 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 2. Amphinemura oblonga Rehman, Du & Zhao sp. nov. A: Male head and prothorax; B: Cervical gills; C: Male terminalia, dorsal view; D: Male terminalia, ventral view.
FIGURE 5 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 5. Amphinemura oblonga Rehman, Du & Zhao sp. nov., male terminalia. A: Dorsal view; B: Ventral view; C: Lateral view; D: Paraproct, oblique view; E: Epiproct, lateral view; F: Epiproct, dorsal view.
FIGURE 3 in Two new species of Amphinemurinae (Plecoptera; Nemouridae) from Yunnan Province, China
FIGURE 3. Amphinemura oblonga Rehman, Du & Zhao sp. nov., male terminalia. A: Lateral view; B: Paraproct, oblique view; C: Epiproct, dorsal view; D–E: Epiproct, ventral view; F: Epiproct, lateral view.
Subspecies and Distribution. G. t. tigrina Schreber, 1776 — South Africa (Southern region of Western Cape to Fastern Cape Provinces). G. t. methi Roberts, 1948 — South Africa (S of Umzigaba River, Pondoland), and Lesotho. in Viverridae
Subspecies and Distribution. G. t. tigrina Schreber, 1776 — South Africa (Southern region of Western Cape to Fastern Cape Provinces). G. t. methi Roberts, 1948 — South Africa (S of Umzigaba River, Pondoland), and Lesotho.
Subspecies and Distribution. L. c. canadensis Schreber, 1776 — E Canada (Maritime Provinces, Ontario & Quebec), NE USA (Maine through New York) and Great Lakes of USA (Michigan and Wisconsin). L. c. kodiacensis Goldman, 1935 — Alaska (Kodiak and Shuyak Is). L. c. lataxina Cuvier, 1823 — E & SE USA. L. c. mira Goldman, 1935 — S Alaska (Prince of Wales I), SW Canada (Vancouver I). L. c. pacifica Rhoads, 1898 — W USA and W Canada. L. c. periclyzomae Elliot, 1905 — W Canada (Queen Charlotte Is). L. c. sonora Rhoads, 1898 — SW USA (Arizona, California, Colorado, Nevada, New Mexico & Utah). in Mustelidae
Subspecies and Distribution. L. c. canadensis Schreber, 1776 — E Canada (Maritime Provinces, Ontario & Quebec), NE USA (Maine through New York) and Great Lakes of USA (Michigan and Wisconsin). L. c. kodiacensis Goldman, 1935 — Alaska (Kodiak and Shuyak Is). L. c. lataxina Cuvier, 1823 — E & SE USA. L. c. mira Goldman, 1935 — S Alaska (Prince of Wales I), SW Canada (Vancouver I). L. c. pacifica Rhoads, 1898 — W USA and W Canada. L. c. periclyzomae Elliot, 1905 — W Canada (Queen Charlotte Is). L. c. sonora Rhoads, 1898 — SW USA (Arizona, California, Colorado, Nevada, New Mexico & Utah).
Subspecies and Distribution. M.b.berezovskiiFlerov,1929—SNingxia,SGansu,SEQuinghai,SShaanxi,WHenan,Sichuan,andSXizang;between500and2500m. M.b.bijiangensisWang&Li,1993—NWYunnantoSEXizang(ZayuCounty). M. b. caobangis Dao, 1969 — S Yunnan (Mile County & Nujiang Langcang), Guangxi, Guangdong, and N Vietnam (Cao Bang Province); between 50 m and 400 m. Presence uncertain in N Laos. M. b. yunguiensis Wang & Ma, 1993 — from the Yunnan-Guizhou plateau margins NE to W Hubei (Yichang). in Moschidae
Subspecies and Distribution. M.b.berezovskiiFlerov,1929—SNingxia,SGansu,SEQuinghai,SShaanxi,WHenan,Sichuan,andSXizang;between500and2500m. M.b.bijiangensisWang&Li,1993—NWYunnantoSEXizang(ZayuCounty). M. b. caobangis Dao, 1969 — S Yunnan (Mile County & Nujiang Langcang), Guangxi, Guangdong, and N Vietnam (Cao Bang Province); between 50 m and 400 m. Presence uncertain in N Laos. M. b. yunguiensis Wang & Ma, 1993 — from the Yunnan-Guizhou plateau margins NE to W Hubei (Yichang).
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear. in Tragulidae
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear.
Subspecies and Distribution. H.b.bruceiGray,1868—Ethiopia. H.b.albipesHollister,1922—Kenya. H.b.bakeriGray,1874—Uganda. H.b.bocageiGray,1869—Angola. H.b.chapiniHatt,1933—DRCongo. H.b.dieseneriBrauer,1917—Tanzania. H.b.fromm:Brauer,1913—Tanzania. H.b.grantiWroughton,1910—SouthAfrica. H.b.hindeiWroughton,1910—Kenya. H.b.hoogstraaliSetzer,1956—Sudan. H.b.kemp:Thomas,1910—Kenya. H.b.lademanniBrauer,1917—Tanzania. H.b.manningiWroughton,1910—Malawi. H.b.mossambicusPeters,1870—Mozambique. H.b.muenzneriBrauer,1913—Tanzania. H.b.princepsThomas,1910—Ethiopia. H.b.prittwitziBrauer,1917—Tanzania. H.b.pumilusThomas,1910—Somaliland. H.b.rudd:Wroughton,1910—Mozambique. H.b.rudolfiThomas,1910—Ethiopia. H.b.somalicusThomas,1892—Somaliland. H.b.ssongeaeBrauer,1917—Tanzania. H.b.thomasiNeumann,1901—Sudan. H. b. victorianjansae Brauer, 1917 — Tanzania. Endemic to Africa from NE Sudan throughout the Horn of Africa, south to Limpopo and Mpumalanga provinces in South Africa, and also isolated populations in Angola. Determining the limits of subspecific distribution is not possible for the moment, but the subspecies and the countries bearing their type localities are included above. in Procaviidae
Subspecies and Distribution. H.b.bruceiGray,1868—Ethiopia. H.b.albipesHollister,1922—Kenya. H.b.bakeriGray,1874—Uganda. H.b.bocageiGray,1869—Angola. H.b.chapiniHatt,1933—DRCongo. H.b.dieseneriBrauer,1917—Tanzania. H.b.fromm:Brauer,1913—Tanzania. H.b.grantiWroughton,1910—SouthAfrica. H.b.hindeiWroughton,1910—Kenya. H.b.hoogstraaliSetzer,1956—Sudan. H.b.kemp:Thomas,1910—Kenya. H.b.lademanniBrauer,1917—Tanzania. H.b.manningiWroughton,1910—Malawi. H.b.mossambicusPeters,1870—Mozambique. H.b.muenzneriBrauer,1913—Tanzania. H.b.princepsThomas,1910—Ethiopia. H.b.prittwitziBrauer,1917—Tanzania. H.b.pumilusThomas,1910—Somaliland. H.b.rudd:Wroughton,1910—Mozambique. H.b.rudolfiThomas,1910—Ethiopia. H.b.somalicusThomas,1892—Somaliland. H.b.ssongeaeBrauer,1917—Tanzania. H.b.thomasiNeumann,1901—Sudan. H. b. victorianjansae Brauer, 1917 — Tanzania. Endemic to Africa from NE Sudan throughout the Horn of Africa, south to Limpopo and Mpumalanga provinces in South Africa, and also isolated populations in Angola. Determining the limits of subspecific distribution is not possible for the moment, but the subspecies and the countries bearing their type localities are included above.
FIGURE 6. Parahystrignathus tongbiguanensis gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 6. Parahystrignathus tongbiguanensis gen. n. et sp. n. Female. SEM images. A: Cephalic end of body; B: Enlarged spines; C: Cephalic end, subapical view; D, E: Cephalic end, en face view, showing cephalic papillae (cp) and amphids (am); F: Vulval region, lateral view, showing the vulva and terminal part of spines; G: A part of body anterior to vulva, showing the posterior part of spines; H: A part of body at excretory pore region, showing the excretory pore and spines near the excretory pore; I: Enlarged image of excretory pore; J: Posterior end of body, showing the anus and tail.
FIGURE 5. Parahystrignathus tongbiguanensis gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 5. Parahystrignathus tongbiguanensis gen. n. et sp. n. Female. A: Anterior part of body, lateral view; B: cephalic end, lateral view (reconstructed from SEM images); C: Whole body, lateral view; D: Posterior end of body, lateral view; E: Cephalic end, en face view (reconstructed from SEM images); F: egg. scale bars: A, C, D, F = 100 μm; B = 30 μm; E = 10 μm.
FIGURE 7 in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 7. Maximum Likelihood (ML) tree inferred from partial sequences of the 28S LSU rDNA of 35 species of Thelastomatoidea. Values of posterior probability and bootstrap (obtained in Bayesian and maximum likelihood analysis, respectively) are shown at the nodes. The sequences obtained from new species are shown in bold font.
FIGURE 2. Huntia morffei gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 2. Huntia morffei gen. n. et sp. n. female. SEM images. A: Cephalic end, en face view, showing cephalic papillae (cp) and amphids (am); B: Cephalic end, lateral view; C: vulva; D: egg.
FIGURE 1. Huntia morffei gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 1. Huntia morffei gen. n. et sp. n. Female. A: Whole body, lateral view; B: Anterior part of body, lateral view; C: Posterior end of body, lateral view; D: cephalic end of body, lateral view; E: egg. scale bars: A, B, C, D, E = 100 μm.
FIGURE 3. Parakongonema sinica gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGURE 3. Parakongonema sinica gen. n. et sp. n. Female. A: Whole body, lateral view; B: Anterior part of body, lateral view; C: Cephalic end of body, lateral view (reconstructed from SEM images); D: posterior end of body, ventral view, showing the lateral alae; E: egg. scale bars: A, B, D = 100 μm, C, E = 50 μm.
Subspecies and Distribution. A. a. azarae Humboldt, 1812 — SC Brazil (Pantanal), S Bolivia (Banados del Izozog), Paraguay (S & W Chaco, W of the Rio Paraguay), and N Argentina (provinces of Chaco & Formosa). A. a. boliviensis Elliot, 1907 — SE Peru (S of the rios Madre de Dios and Inambari) and Bolivia E of the Andes (from the Rio Madre de Dios S to the Banados del Izozog in the border region with Paraguay). A. a. infulatus Kuhl, 1820 — Brazil, S of the Rio Amazonas (but with a small enclave in the SE tip of Amapa State), including Marajo and Caviana Is, extending E in the state of Maranhao as far as the Rio Parnaiba, S along the W bank of Rio Tocantins to the Pantanal of Mato Grosso, W limits are marked by the rios Tapajos and Juruena. in Aotidae
Subspecies and Distribution. A. a. azarae Humboldt, 1812 — SC Brazil (Pantanal), S Bolivia (Banados del Izozog), Paraguay (S & W Chaco, W of the Rio Paraguay), and N Argentina (provinces of Chaco & Formosa). A. a. boliviensis Elliot, 1907 — SE Peru (S of the rios Madre de Dios and Inambari) and Bolivia E of the Andes (from the Rio Madre de Dios S to the Banados del Izozog in the border region with Paraguay). A. a. infulatus Kuhl, 1820 — Brazil, S of the Rio Amazonas (but with a small enclave in the SE tip of Amapa State), including Marajo and Caviana Is, extending E in the state of Maranhao as far as the Rio Parnaiba, S along the W bank of Rio Tocantins to the Pantanal of Mato Grosso, W limits are marked by the rios Tapajos and Juruena.
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department). in Atelidae
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department).
Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus. in Atelidae
Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus.
FIGUR 4. Parakongonema sinica gen. n in Three new genera and new species of hystrignathid nematodes (Nematoda: Thelastomatoidea) from passalid beetles (Insecta: Passalidae) from Yunnan Province, China with phylogenetic analysis of Hystrignathidae
FIGUR 4. Parakongonema sinica gen. n. et sp. n. Female. SEM images. A: Whole body, lateral view, showing a lateral ala; B: Cephalic end, subapical view, showing cephalic papillae (cp) and amphids (am); C: Anterior part of body, ventral view, showing beginning of lateral alae and excretory pore (ep); D: Enlarged image of excretory pore; E: Posterior end of body
Distribution. Endemic to SW Africa; known to occurin scattered areas from type locality on SW coast of Angola S across W Namibia to N parts of Northern Cape Province in South Africa. in Cistugidae
Distribution. Endemic to SW Africa; known to occurin scattered areas from type locality on SW coast of Angola S across W Namibia to N parts of Northern Cape Province in South Africa.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.